Canonical Allele Identifier: CA355011998
Gene: CLRN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.150972585T>A , CM000665.2:g.150972585T>A GRCh38
NC_000003.11:g.150690372T>A , CM000665.1:g.150690372T>A GRCh37
NC_000003.10:g.152173062T>A NCBI36
NG_009168.1:g.5415A>T , LRG_700:g.5415A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000327047.6:c.124A>T MANE Select ENSP00000322280.1:p.Thr42Ser
ENST00000468836.2:c.100A>T ENSP00000419892.2:p.Thr34Ser
ENST00000327047.5:c.124A>T ENSP00000322280.1:p.Thr42Ser
ENST00000328863.8:c.124A>T ENSP00000329158.4:p.Thr42Ser
ENST00000468836.1:c.-277A>T ENSP00000419892.1:n.-277A>T
ENST00000472224.1:n.130A>T
NM_001195794.1:c.124A>T , LRG_700t1:c.124A>T NP_001182723.1:p.Thr42Ser
NM_001256819.1:c.124A>T NP_001243748.1:p.Thr42Ser
NM_174878.2:c.124A>T NP_777367.1:p.Thr42Ser
NR_046380.2:n.415A>T
XR_924167.1:n.436A>T
NM_001256819.2:c.124A>T NP_001243748.1:p.Thr42Ser
NM_174878.3:c.124A>T MANE Select NP_777367.1:p.Thr42Ser
NR_046380.3:n.143A>T